加油站地下储油罐压力管理系统的相关研究

在当前普遍采用的加油站真空辅助式第二阶段油气回收系统中,为了避免回收到地下储油罐中的油气再次通过P/V阀排空,必须对其中气相空间的压力实施有效控制。从国外的发展情况来看,地下储油罐的压力管理系统主要分为基于膜分离技术、基于弹性气囊和基于活性炭吸附三大类,其中膜法油气回收装置在国内已经得到了较多关注。首次系统介绍了气囊式压力管理系统的工作原理及其主要结构设计,具体包括管线布局、钢制压力容器壳体、位于容器顶部封头上的接口组件和全部位于容器内的气囊等;同时对另外一种可行方案进行了分析。     

改性氧化铝微波诱导催化氧化处理高浓度苯酚废水的研究

采用微波诱导催化氧化技术,以改性氧化铝为催化剂,对高浓度模拟苯酚废水进行氧化处理。考察了微波功率、催化剂投加量、H202投加量、废水pH值和微波反应时间等因素对苯酚去除效果的影响。实验结果表明,处理30mL质量浓度为1 100mg/L的苯酚模拟废水,在微波功率500W,催化剂加入量1 g(液固比30∶1),30％双氧水...     

Elevated atmospheric deposition and dynamics of mercury in a remote upland forest of southwestern China

Mt. Gongga area in southwest China was impacted by Hg emissions from industrial activities and coal combustion, and annual means of atmospheric TGM and PHg concentrations at a regional background station were 3.98 ng m⁻³ and 30.7 pg m⁻³, respectively. This work presents a mass balance study of Hg in an upland forest in this area. Atmospheric deposition was highly elevated in the study area, with the annual mean THg deposition flux of 92.5 μg m⁻² yr⁻¹. Total deposition was dominated by dry deposition (71.8%), and wet deposition accounted for the remaining 28.2%. Forest was a large pool of atmospheric Hg, and nearly 76% of the atmospheric input was stored in forest soil. Volatilization and stream outflow were identified as the two major pathways for THg losses from the forest, which yielded mean output fluxes of 14.0 and 8.6 μg m⁻² yr⁻¹, respectively.     

Nationwide monitoring of atmospheric PCDD/Fs and dioxin-like PCBs in South Korea

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) were measured in ambient air samples collected from different parts of South Korea in 2008, and the measured levels were used for assessing the spatial and temporal distribution of atmospheric PCDDFs and DL-PCBs in South Korea. The average concentrations of atmospheric PCDD/Fs and DL-PCBs among the 37 sites were 28 fg I-TEQ m⁻³ (ND ∼ 617) and 1 fg WHO-TEQ m⁻³ (ND ∼ 0.016). Elevated atmospheric levels of PCDD/Fs and DL-PCBs observed at residential/industrial sites and in the north-west of Korea, indicated a potential contribution and impacts of anthropogenic sources of PCDD/Fs and DL-PCBs. These levels were similar or lower than those previously reported in other ambient air surveys. Average concentrations of PCDD/Fs showed small seasonal variations (ANOVA analysis, p = 0.144). The highest concentrations of PCDD/Fs were observed during winter, followed by spring, autumn and summer. Atmospheric PCDD/Fs and DL-PCBs in South Korea rapidly decreased during the last 10 years (1998-2008), demonstrating the efficiency of stricter regulations and the application of best available technologies/best environmental practices at emission sources. Comparison of the congener profiles and principal component analysis showed that current atmospheric PCDD/Fs are mostly influenced by industrial sources and PCBs from old commercial PCB uses. Nationwide POPs monitoring will continue and allows an effective evaluation of the implementation of the Stockholm Convention on POPs.     

不同混凝剂处理松花江低温水

东北松花江地区冬季有将近6个月的冰封期,低温季节水源水处理难度大。为了保证东北地区冬季饮用水供应,研究几种混凝剂在处理冬季松花江低温水时的混凝效果。实验结果表明,NPAC1和NPAC2水解产物中具有较高的Alb和Alc成分,拥有较高的电中和、吸附和网捕卷扫性能,高效聚铝铁(PAF)水解产物Fe(OH)3具有比表面积大、吸附架桥作用较强的优点。这3种混凝剂无论是在控制出水浊度还是在对水体有机物去除能力方面均优于目前水厂所使用的PAC和聚合氯化铝铁(水厂PAF);NPAC2的投加量达到50 mg/L时,出水浊度达到最优;当混凝剂投加量达到50 mg/L时,NPAC1的浊度去除率逐渐超过NPAC2,剩余浊度低于3.0 NTU;NPAC1、NPAC2和PAF 3种混凝剂对有机物的去除能力大致相当,当混凝剂投加量为50 mg/L时,这3种混凝剂处理后的水的UV254的值均低于0.06,而水厂使用的2种混凝剂处理后的水的UV254仍高于0.1;结合其对浊度去除的情况,可以判断55 mg/L的投药量为NPAC1的最优投药点,PAF的最佳投药量为65 mg/L;投加适量的粉末活性碳可以有效地提高氨氮的去除率,当粉末活性炭的投加量为30 mg/L时,氨氮的去除率基本达到最大(51.27%)。表面负荷对混凝效果具有重要的影响,合理降低沉淀池的表面负荷对于提高出水水质具有重要作用。     

Predicting the bioavailability of sediment-associated polybrominated diphenyl ethers using a 45-d sequential Tenax extraction

A 45-d Tenax extraction was used to evaluate the bioavailability of polybrominated diphenyl ethers (PBDEs) in three spiked sediments. The effect of aging on desorption kinetics of PBDEs was investigated by incubating one of the sediments for 7, 14, 30 and 60 d at room temperature. Desorption kinetics were well described by a three-compartment model. The fraction of very slow desorption (Fvs) contributed the most of the desorbed PBDEs from sediments. The total desorption amount of PBDEs decreased with the increase of total organic carbon in the sediments, suggesting that organic matter is an important factor controlling the partition of PBDEs in sediments. The total desorption amount of PBDEs decreased while log [(Fslow+Fvs)/Frap] increased with logKow of PBDE congeners, indicating that the bioavailability of PBDEs in sediment decreases with logKow of the congeners. As the residential time of PBDEs in the sediment increased from 7 to 60 d, Frap of individual PBDE congeners decreased gradually with simultaneous increase of Fvs. There was a good positive correlation between Frap and F6/F24, indicating that either 6 h or 24 h Tenax extraction could be a proxy for Frap and bioavailability. In general, the results in present study suggest that the bioavailability of nona- and deca-BDEs in sediment is very low due to their strong hydrophobicity and large molecular size.     

Efficiency of surfactant-enhanced desorption for contaminated soils depending on the component characteristics of soil-surfactant--PAHs system

The sorption of surfactants onto soils has a significant effect on the performance of surfactant enhanced desorption. In this study, the efficiency of surfactants in enhancing desorption for polycyclic aromatic hydrocarbons (PAHs) contaminated soils relative to water was evaluated with a term of relative efficiency coefficient (REC). Since the sorption of surfactants onto soils, surfactants only enhanced PAH desorption when REC values were larger than 1 and the added surfactant concentration was greater than the corresponding critical enhance desorption concentration (CEDC), which was defined as the corresponding surfactant concentration with REC=1. A model was utilized to describe and predict the REC and CEDC values for PAH desorption. The model and experimental results indicated that the efficiency of surfactants in enhancing PAH desorption showed strong dependence on the soil composition, surfactant structure and PAH properties. These results are of practical interest for the selection of surfactant to optimize soil remediation technologies.     

企业安全管理信息系统的总体构建

通过对安全管理现状的调查研究,根据现行企业安全管理系统的实际情况和问题进行安全管理信息系统的总体构建.此系统可以解决目前企业安全管理中普遍存在的问题如安全信息缺乏,信息渠道不畅通,反馈不及时等.因此,对企业向着安全管理方面发展具有十分重要的现实意义.     

Size distributions of aerosol and water-soluble ions in Nanjing during a crop residual burning event

To investigate the impact on urban air pollution by crop residual burning outside Nanjing, aerosol concentration, pollution gas concentration, mass concentration, and water-soluble ion size distribution were observed during one event of November 4-9, 2010. Results show that the size distribution of aerosol concentration is bimodal on pollution days and normal days, with peak values at 60-70 and 200-300 nm, respectively. Aerosol concentration is 10⁴ cm^-3. nm^-1 on pollution days. The peak value of spectrum distribution of aerosol concentration on pollution days is 1.5-3.3 times higher than that on a normal day. Crop residual burning has a great impact on the concentration of fine particles. Diurnal variation of aerosol concentration is trimodal on pollution days and normal days, with peak values at 03:00, 09:00 and 19:00 local standard time. The first peak is impacted by meteorological elements, while the second and third peaks are due to human activities, such as rush hour traffic. Crop residual burning has the greatest impact on SO₂ concentration, followed by NO₂, O₃ is hardly affected. The impact of crop residual burning on fine particles (< 2.1 μm) is larger than on coarse particles (> 2.1 μm), thus ion concentration in fine particles is higher than that in coarse particles. Crop residual burning leads to similar increase in all ion components, thus it has a small impact on the water-soluble ions order. Crop residual burning has a strong impact on the size distribution of K⁺, Cl^-, Na⁺, and F^- and has a weak impact on the size distributions of NH₄⁺, Ca²⁺, NO₃^- and SO₄^2-.     

Removal of polycyclic aromatic hydrocarbons and phenols from coking wastewater by simultaneously synthesized organobentonite in a one-step process

The optimal condition for a one-step process removing organic compounds from coking wastewater by simultaneously synthesized organobentonite as a pretreatment was investigated. Results showed that sorption of organic compounds by organobentonite was positively correlated to the cation surfactant exchange on the bentonite and the octanol-water partition coefficient (K_ow) of the solutes. With 0.75 g/L bentonite and 180 mg/L (60% of bentonite cation exchange capacity) cetyltrimethylammonium bromide, the removal efficiencies of the 16 polycyclic aromatic hydrocarbon (PAHs) specified by the US Environmental Protection Agency in coking wastewater except naphthalene were more than 90%, and that of benzo(a)pyrene was 99.5%. At the same time, the removal efficiencies of COD_Cr, NH₃-N, volatile phenols, colour and turbidity were 28.6%, 13.2%, 8.9%, 55% and 84.3%, respectively, and the ratio of BOD₅/COD_Cr increased from 0.31 to 0.41. These results indicated that the one-step process had high removal efficiency for toxic and refractory hydrophobic organic compounds, and could improve the biodegradability of the coking wastewater. Therefore it could be a promising technology for the pretreatment of toxic and refractory organic wastewater.